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Clinical Trials/NCT03201575
NCT03201575
Completed
N/A

REmote Ischemic COnditioning in Septic Shock: The RECO-Sepsis Study

Hospices Civils de Lyon6 sites in 1 country180 target enrollmentNovember 28, 2017
ConditionsSeptic Shock

Overview

Phase
N/A
Intervention
Not specified
Conditions
Septic Shock
Sponsor
Hospices Civils de Lyon
Enrollment
180
Locations
6
Primary Endpoint
Average SOFA score (Sequential Organ Failure Assessment)
Status
Completed
Last Updated
5 months ago

Overview

Brief Summary

Septic shock remains a major public health problem in industrialized countries, with a mortality rate as high as 50%, largely related to multiple organ dysfunction. In addition to dysregulated inflammatory response, the pathophysiology of organ failures in septic shock involves ischemia-reperfusion processes. Remote ischemic conditioning is a therapeutic strategy for protecting organs against the detrimental effects of ischemia-reperfusion injury.

The objective of the present study is to determine whether remote ischemic conditioning can limit the severity of organ failure in patients with septic shock.

Registry
clinicaltrials.gov
Start Date
November 28, 2017
End Date
August 12, 2019
Last Updated
5 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Age ≥ 18 years
  • Hospitalization in an intensive care unit for less than 24 hours
  • Septic shock evolving for less than 12 hours defined as:
  • Documented or suspected infection
  • Norepinephrine administration to maintain a mean arterial pressure ≥ 65 mmHg after volemia correction
  • Lactatemia \> 2 mmol/L at least once in the past 12 hours before inclusion
  • Written informed consent signed by the patient or by a next of kin or oral consent given by the patient and as soon as permitted by the clinical state written informed consent signed by the patient.

Exclusion Criteria

  • Patient who has expressed the wish not to be resuscitated
  • Contraindication of the use of brachial cuff on both arms
  • Intercurrent pathology with an expected life expectancy of less than 24 hours
  • Cardiac arrest
  • Female patients currently pregnant or women of childbearing age who are not using contraception
  • Previous inclusion in RECO-Sepsis study
  • Previous inclusion in another clinical study
  • Patients without health coverage

Outcomes

Primary Outcomes

Average SOFA score (Sequential Organ Failure Assessment)

Time Frame: 96 hours.

The SOFA score ranges from 0 to 24 (higher scores indicate more severe organ failure), with 0 to 4 points assigned for each of 6 organ dysfunctions (ie, central nervous system, cardiovascular, respiratory, renal, coagulation, and liver).

Secondary Outcomes

  • Hospital length of stay(Day 90)
  • All-cause mortality(Day 90)
  • Average SOFA score without the neurologic sub-score.(96 hours.)
  • SOFA score.(96 hours)
  • Variations of SOFA score (delta-SOFA)(24 hours)
  • SOFA sub-scores for each organs(96 hours)
  • Survival without organ support(Day 28)
  • Intensive care unit (ICU) length of stay.(Day 90)

Study Sites (6)

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